Product image of Glucosio Bioindustria L.I.M. (Glucose Monohydrate) supplied by GNH India

Glucosio Bioindustria L.I.M.

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucosio Bioindustria L.I.M. (Glucose Monohydrate)

Glucosio Bioindustria L.I.M. is a parenteral carbohydrate solution that contains glucose monohydrate as its sole active ingredient. It is supplied in an injectable form for intramuscular or intravenous administration and complies with European Union pharmaceutical standards. The product delivers a readily available source of glucose to support cellular energy metabolism in clinical settings where rapid carbohydrate supplementation is needed, and it is provided in sterile containers for controlled use.

Manufacturer / TM Owner

Bioindustria Lim Laboratorio Italiano Medicinali Spa

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Indications & Clinical Uses

Glucosio Bioindustria L.I.M. is used as an immediate source of carbohydrate in various medical situations that require rapid energy provision or maintenance of blood glucose levels.

  • Intravenous or intramuscular supplementation of glucose in patients undergoing surgery or anesthesia.
  • Management of hypoglycemia when oral intake is not feasible.
  • Provision of caloric support in critically ill or trauma patients.
  • Support of metabolic needs during parenteral nutrition regimens.
  • Replacement of fluid and electrolyte losses associated with glucose depletion.

Side Effects

The safety profile of Glucosio Bioindustria L.I.M. reflects the expected pharmacologic actions of glucose administered intravenously or intramuscularly.

Common

  • Transient hyperglycemia
  • Local irritation at the injection site
  • Mild nausea
  • Headache
  • Temporary increase in serum osmolality

Serious

  • Severe hyperglycemia leading to osmotic diuresis
  • Allergic or anaphylactic reaction
  • Hyperosmolar hyperglycemic state
  • Metabolic acidosis in predisposed patients
  • Venous thrombosis related to infusion

Precautions & Warnings

When using Glucosio Bioindustria L.I.M., clinicians should consider several precautionary measures to ensure safe administration.

  • Verify patient’s blood glucose level before and after infusion.
  • Adjust dose in patients with renal or hepatic impairment.
  • Use caution in individuals with diabetes mellitus or insulin resistance.
  • Monitor electrolyte balance, especially sodium and potassium, during large-volume administration.
  • Avoid rapid infusion rates to reduce risk of circulatory overload.
  • Ensure aseptic technique to prevent infection at the injection site.
  • Review concurrent carbohydrate intake to prevent excess caloric load.

Avoid Interactions

Glucose solutions can interact with other medications or clinical conditions; awareness of these interactions helps optimize therapy.

Avoid

  • Concurrent administration of high-dose insulin without glucose monitoring.
  • Use with hyperosmolar agents that may exacerbate fluid shifts.
  • Co-administration with drugs that cause hypoglycemia (e.g., sulfonylureas) without adjustment.

Use with caution

  • Beta‑blockers, which may mask hypoglycemia symptoms.
  • Diuretics that alter electrolyte status.
  • Corticosteroids that increase glucose production.
  • Catecholamines or glucagon that raise blood glucose levels.
  • Total parenteral nutrition formulations containing additional carbohydrates.

Frequently Asked Questions

The product contains glucose monohydrate as its sole active ingredient.

Yes, it is formulated for both intravenous (IV) and intramuscular (IM) injection routes.

It is commonly used for rapid carbohydrate supplementation during surgery, to treat hypoglycemia, and as part of parenteral nutrition in critically ill patients.

Blood glucose levels should be checked before and after administration, and electrolytes should be monitored during large-volume infusions.

It can be used in diabetic patients, but dosage and infusion rate should be carefully adjusted and glucose levels closely monitored.

Common side effects include transient hyperglycemia, mild nausea, headache, local irritation at the injection site, and temporary changes in serum osmolality.

Serious reactions may include severe hyperglycemia, allergic or anaphylactic responses, hyperosmolar hyperglycemic state, metabolic acidosis, or infusion‑related thrombosis.

Mixing is generally discouraged unless compatibility has been confirmed; incompatibility can affect drug stability and patient safety.

Renal impairment may reduce glucose clearance, so dose reduction and close monitoring of blood glucose and electrolytes are recommended.

The solution should be stored in a controlled‑temperature environment, protected from light, and used before the expiration date indicated on the packaging.

Use in children is possible but requires weight‑based dosing and careful monitoring; consult pediatric dosing guidelines.

The product is classified under ATC code A12AA01, which corresponds to simple sugars used as parenteral carbohydrate solutions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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